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  Satb2 Is Required for the Development of a Spinal Exteroceptive Microcircuit that Modulates Limb Position

Hilde, K. L., Levine, A. J., Hinckley, C. A., Montgomery, J. M., Gullo, M., Driscoll, S. P., et al. (2016). Satb2 Is Required for the Development of a Spinal Exteroceptive Microcircuit that Modulates Limb Position. Neuron, 91, 763-776. doi:10.1016/j.neuron.2016.07.014.

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Hilde, Kathryn L.1, Author
Levine, Ariel J.1, Author
Hinckley, Christopher A.1, Author
Montgomery, Jessica M.1, Author
Gullo, Miriam1, Author
Driscoll, Shawn P.1, Author
Grosschedl, Rudolf2, Author           
Kohwi, Yoshinori1, Author
Kohwi-Shigematsu, Terumi1, Author
Pfaff, Samuel1, Author
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1External Organizations, ou_persistent22              
2Department of Cellular and Molecular Immunology, Max Planck Institute of Immunobiology and Epigenetics, Max Planck Society, ou_2243641              

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 Abstract: Motor behaviors such as walking or withdrawing the limb from a painful stimulus rely upon integrative multimodal sensory circuitry to generate appropriate muscle activation patterns. Both the cellular components and the molecular mechanisms that instruct the assembly of the spinal sensorimotor system are poorly understood. Here we characterize the connectivity pattern of a sub-population of lamina V inhibitory sensory relay neurons marked during development by the nuclear matrix and DNA binding factor Satb2 (ISR(Satb2)). ISR(Satb2) neurons receive inputs from multiple streams of sensory information and relay their outputs to motor command layers of the spinal cord. Deletion of the Satb2 transcription factor from ISR(Satb2) neurons perturbs their cellular position, molecular profile, and pre- and post-synaptic connectivity. These alterations are accompanied by abnormal limb hyperflexion responses to mechanical and thermal stimuli and during walking. Thus, Satb2 is a genetic determinant that mediates proper circuit development in a core sensory-to-motor spinal network.

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Language(s): eng - English
 Dates: 2016-08-17
 Publication Status: Published online
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 Rev. Type: Peer
 Identifiers: DOI: 10.1016/j.neuron.2016.07.014
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Title: Neuron
Source Genre: Journal
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Publ. Info: Cambridge, Mass. : Cell Press
Pages: - Volume / Issue: 91 Sequence Number: - Start / End Page: 763 - 776 Identifier: ISSN: 0896-6273
CoNE: https://pure.mpg.de/cone/journals/resource/954925560565